Our specialist team of senior-level pharmaceutical industry experts has a proven track record of successfully supporting companies worldwide throughout their medicinal product and medical device development lifecycle.
Our team of pharmaceutical consultants understands the requirements of each phase and aspect of medicinal/device development and regulatory approval across therapeutic areas and product/device types.
We consult on non-clinical, clinical, strategic development, and product safety issues.
We have over two decades of proven success in providing effective solutions to the global pharmaceutical, biotechnology, and medical device sectors.
Our specialist team of pharmaceutical consultants offer scientific expertise, specialised knowledge, and experience across all phases of medicinal product development and the intricacies of regulatory compliance (EMA, MHRA, FDA) from non-clinical to regulatory approval.
Examples:
General Sales List, pharmacy only, prescription only, controlled drugs.
Do you need timely, accurate, and up-to-date advice regarding the diverse and sometimes confusing license applications and regulatory approval processes?
Our experts can help you avoid unnecessary launch delays and ensure you meet regulatory requirements.
Examples:
Biological products, including vaccines, blood and blood components, allergenics, somatic cells, gene therapy, tissues, and recombinant therapeutic proteins. Any biosimilar or interchangeable biosimilar medicine.
Advanced therapy medicinal products (ATMPs) face several challenges during development, approval and postmarketing, including uncertainty about the product's benefit-risk balance, limitations of nonclinical development, and complex quality aspects of highly individualised advanced therapies.
We have in-depth knowledge and expertise in the regulatory approval processes for innovative therapies that mainly target orphan diseases and high unmet medical needs.
Do you need help building a pharmacovigilance or medical device vigilance programme grounded in quality, compliance and efficiency to ensure patient safety is central to your development?
We can provide an outsourced vigilance department with product safety specialists and physicians utilising a state-of-the-art vigilance database to process safety reports and ensure compliance with regulatory agency requirements, including FDA and EMA.
We can prepare and submit aggregate reports, such as the DSUR.
We can act as your QPPV or Eudravigilance Responsible Person.
We have successfully troubleshooted difficult regulatory issues, particularly EMA Articles 20 and 31.